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Gaceta Medica De Mexico|February 8, 2018
Epidemiología genética sobre las teorías causales y la patogénesis de la diabetes mellitus tipo 2Carlos Jonnathan Castro-Juárez, Sergio Alberto Ramírez-García, Nemesio Villa-Ruano, et al.
Gaceta Medica De Mexico|February 26, 2019
[Ataxina-2, nuevo blanco en enfermedades genéticas complejas]Sergio Alberto Ramírez-García, José Sánchez-Corona, Diego Ortega-Pacheco, et al.
American Journal of Medical Genetics. Part A|April 1, 2005
Mental retardation in a boy with anterior cervical hypertrichosisJ Román Corona-Rivera, Sergio González-Abarca, Juan Hernández-Rocha, et al.
Gaceta Medica De Mexico|February 25, 2020
Genetic approach in amyotrophic lateral sclerosisIván Cervantes-Aragón, Sergio Alberto Ramírez-García, Luz Margarita Baltazar-Rodríguez, et al.
Gaceta Medica De Mexico|November 8, 2019
Aproximación genética en la esclerosis lateral amiotróficaIván Cervantes-Aragón, Sergio Alberto Ramírez-García, Luz Margarita Baltazar-Rodríguez, et al.
American Journal of Medical Genetics|January 25, 2002
Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomesNancy Monroy, Marisol López, Alicia Cervantes, et al.
American Journal of Medical Genetics. Part A|April 6, 2005
Split hand malformation, hypospadias, microphthalmia, distinctive face and short stature in two brothers suggest a new syndromeJose E García-Ortiz, Felipe Banda-Espinoza, Juan C Zenteno, et al.
Clinical Dysmorphology|December 13, 2006
Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: a new familial faciocardiomelic syndrome?José Elías García-Ortiz, Diana García-Cruz, Ingrid Patricia Dávalos, et al.
Archivos Argentinos De Pediatria|September 9, 2016
[Anterior cervical hypertrichosis: case report]Mario H Orozco-Gutiérrez, José Sánchez-Corona, José E García-Ortiz, et al.
American Journal of Medical Genetics. Part A|November 5, 2003
Chromosome instability induced in vitro with mitomycin C in five Seckel syndrome patientsLucina Bobabilla-Morales, Alfredo Corona-Rivera, J Román Corona-Rivera, et al.
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